UDI device identifier

Allied Medical LLC 0V000001

UDI device identifier 00026072000182 · Allied Medical, LLC

Key facts

Primary DI 00026072000182
Brand name Allied Medical LLC
Version or model 0V000001
Catalog number D81
Company Allied Medical, LLC
DUNS number 119066872
Product code CBK
GMDN term Pulmonary resuscitator, pneumatic, reusable
Premarket submission K872113
Device class Class II
Single use No
Packaged sterile No
Implantable No
Publish date Nov 20, 2015
Version date Oct 13, 2025
Description Ventilator, Omni-Vent, D-8 MRI compatible control unit.

At a glance

  • None MAUDE reports citing this UDI
  • Yes Linked premarket submission
  • No EUDAMED counterpart found
  • 1,000+ GUDID devices with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About UDI device identifiers (GUDID)

The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.

Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date:

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